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Items: 1 to 20 of 99

1.

Mannose-6-phosphate regulates destruction of lipid-linked oligosaccharides.

Gao N, Shang J, Huynh D, Manthati VL, Arias C, Harding HP, Kaufman RJ, Mohr I, Ron D, Falck JR, Lehrman MA.

Mol Biol Cell. 2011 Sep;22(17):2994-3009. doi: 10.1091/mbc.E11-04-0286. Epub 2011 Jul 7.

2.

Mannose-6-phosphate: a regulator of LLO destruction.

Gao N, Lehrman MA.

Methods Mol Biol. 2013;1022:277-82. doi: 10.1007/978-1-62703-465-4_20.

PMID:
23765668
4.

A zebrafish model of PMM2-CDG reveals altered neurogenesis and a substrate-accumulation mechanism for N-linked glycosylation deficiency.

Cline A, Gao N, Flanagan-Steet H, Sharma V, Rosa S, Sonon R, Azadi P, Sadler KC, Freeze HH, Lehrman MA, Steet R.

Mol Biol Cell. 2012 Nov;23(21):4175-87. doi: 10.1091/mbc.E12-05-0411. Epub 2012 Sep 5.

5.

Translation attenuation by PERK balances ER glycoprotein synthesis with lipid-linked oligosaccharide flux.

Shang J, Gao N, Kaufman RJ, Ron D, Harding HP, Lehrman MA.

J Cell Biol. 2007 Feb 26;176(5):605-16.

8.

Glucosamine induces ER stress by disrupting lipid-linked oligosaccharide biosynthesis and N-linked protein glycosylation.

Beriault DR, Dang VT, Zhong LH, Petlura CI, McAlpine CS, Shi Y, Werstuck GH.

Am J Physiol Endocrinol Metab. 2017 Jan 1;312(1):E48-E57. doi: 10.1152/ajpendo.00275.2016. Epub 2016 Nov 22.

10.

Analysis and metabolic engineering of lipid-linked oligosaccharides in glycosylation-deficient CHO cells.

Jones MB, Tomiya N, Betenbaugh MJ, Krag SS.

Biochem Biophys Res Commun. 2010 Apr 23;395(1):36-41. doi: 10.1016/j.bbrc.2010.03.117. Epub 2010 Mar 21.

11.

Exogenous mannose does not raise steady state mannose-6-phosphate pools of normal or N-glycosylation-deficient human fibroblasts.

Higashidani A, Bode L, Nishikawa A, Freeze HH.

Mol Genet Metab. 2009 Apr;96(4):268-72. doi: 10.1016/j.ymgme.2008.12.005. Epub 2009 Jan 20.

14.

Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts.

Eklund EA, Merbouh N, Ichikawa M, Nishikawa A, Clima JM, Dorman JA, Norberg T, Freeze HH.

Glycobiology. 2005 Nov;15(11):1084-93. Epub 2005 Aug 3.

PMID:
16079417
15.

Identification of phosphorylated oligosaccharides in cells of patients with a congenital disorders of glycosylation (CDG-I).

Vleugels W, Duvet S, Peanne R, Mir AM, Cacan R, Michalski JC, Matthijs G, Foulquier F.

Biochimie. 2011 May;93(5):823-33. doi: 10.1016/j.biochi.2011.01.016. Epub 2011 Feb 16.

PMID:
21315133
17.

Mammalian STT3A/B oligosaccharyltransferases segregate N-glycosylation at the translocon from lipid-linked oligosaccharide hydrolysis.

Lu H, Fermaintt CS, Cherepanova NA, Gilmore R, Yan N, Lehrman MA.

Proc Natl Acad Sci U S A. 2018 Sep 18;115(38):9557-9562. doi: 10.1073/pnas.1806034115. Epub 2018 Sep 4.

18.

A partial deficiency of dehydrodolichol reduction is a cause of carbohydrate-deficient glycoprotein syndrome type I.

Ohkura T, Fukushima K, Kurisaki A, Sagami H, Ogura K, Ohno K, Hara-Kuge S, Yamashita K.

J Biol Chem. 1997 Mar 14;272(11):6868-75.

19.

Protein kinase R-like endoplasmic reticulum kinase and glycogen synthase kinase-3α/β regulate foam cell formation.

McAlpine CS, Werstuck GH.

J Lipid Res. 2014 Nov;55(11):2320-33. doi: 10.1194/jlr.M051094. Epub 2014 Sep 2.

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